Canonical Allele Identifier: CA1949577183
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5254274A= , CM000673.2:g.5254274A= GRCh38
NC_000011.9:g.5275504A= , CM000673.1:g.5275504A= GRCh37
NC_000011.8:g.5232080A= NCBI36
NG_000007.3:g.43342T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336906.6:c.315+18T= MANE Select ENSP00000338082.4:n.315+18T=
ENST00000380252.6:c.150+18T= ENSP00000369602.2:n.150+18T=
ENST00000642908.1:c.315+18T= ENSP00000495346.1:n.315+18T=
ENST00000647543.1:c.315+18T= ENSP00000496470.1:n.315+18T=
ENST00000336906.4:c.315+18T= ENSP00000338082.4:n.315+18T=
ENST00000380252.5:c.285+18T= ENSP00000369602.1:n.285+18T=
ENST00000380259.6:c.315+18T= ENSP00000369609.2:n.315+18T=
ENST00000444587.1:c.*184+18T= ENSP00000488218.1:n.*184+18T=
ENST00000620888.4:c.315+18T= ENSP00000479637.1:n.315+18T=
ENST00000624109.1:c.43-21A= ENSP00000485458.1:n.43-21A=
NM_000184.2:c.315+18T= NP_000175.1:n.315+18T=
NM_000184.3:c.315+18T= MANE Select NP_000175.1:n.315+18T=